Papers associated with LOC105447179

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	Congenital heart disease in children: Orofacial myofunctional aspects, eating behavior and facial temperature., Barbosa MDG, Castelo PM, Ferreira CLP, Haddad DS, Chiari BM, Santana MV, Bommarito S., Int J Pediatr Otorhinolaryngol. April 1, 2020; 131 109883.
	Xenbase: Facilitating the Use of Xenopus to Model Human Disease., Nenni MJ, Fisher ME, James-Zorn C, Pells TJ, Ponferrada V, Chu S, Fortriede JD, Burns KA, Wang Y, Lotay VS, Wang DZ, Segerdell E, Chaturvedi P, Karimi K, Vize PD, Zorn AM., Front Physiol. February 26, 2019; 10 154.
	WDR5 regulates left-right patterning via chromatin-dependent and -independent functions., Kulkarni SS, Khokha MK., Development. November 28, 2018; 145 (23):
	RPSA, a candidate gene for isolated congenital asplenia, is required for pre-rRNA processing and spleen formation in Xenopus., Griffin JN, Sondalle SB, Robson A, Mis EK, Griffin G, Kulkarni SS, Deniz E, Baserga SJ, Khokha MK., Development. October 18, 2018; 145 (20):
	Single nucleotide editing without DNA cleavage using CRISPR/Cas9-deaminase in the sea urchin embryo., Shevidi S, Uchida A, Schudrowitz N, Wessel GM, Yajima M., Dev Dyn. December 1, 2017; 246 (12): 1036-1046.
	Analysis of Craniocardiac Malformations in Xenopus using Optical Coherence Tomography., Deniz E, Jonas S, Hooper M, N Griffin J, Choma MA, Khokha MK., Sci Rep. February 14, 2017; 7 42506.
	Proteolytic processing of von Willebrand factor by adamts13 and leukocyte proteases., Lancellotti S, Basso M, De Cristofaro R., Mediterr J Hematol Infect Dis. September 2, 2013; 5 (1): e2013058.
	Shells and heart: are human laterality and chirality of snails controlled by the same maternal genes?, Oliverio M, Digilio MC, Versacci P, Dallapiccola B, Marino B., Am J Med Genet A. October 1, 2010; 152A (10): 2419-25.
	Starfish-assisted off-pump obliteration of massive coronary arteriovenous fistulae., Sun S, Li JY, Hu PY, Wu SJ., Tex Heart Inst J. January 1, 2005; 32 (4): 595-7.
	Isolation of a novel human homologue of the gene coding for echinoderm microtubule-associated protein (EMAP) from the Usher syndrome type 1a locus at 14q32., Eudy JD, Ma-Edmonds M, Yao SF, Talmadge CB, Kelley PM, Weston MD, Kimberling WJ, Sumegi J., Genomics. July 1, 1997; 43 (1): 104-6.
	Keratoderma hereditarium mutilans (Vohwinkel''s syndrome) associated with congenital deaf-mutism., Peris K, Salvati EF, Torlone G, Chimenti S., Br J Dermatol. April 1, 1995; 132 (4): 617-20.

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